In situ iron isotope ratios (δ 56 Fe) in sulfide measured by secondary ion mass spectrometry (SIMS) can provide valuable information on several of Earth's surface processes. SIMS relies on the use of a matrix‐matched reference material to correct for instrumental mass fractionation. To date Balmat pyrite has been widely used as a reference material, on the assumption of its homogeneous δ 56 Fe composition. However, several studies have reported divergent bulk δ 56 Fe values, which may jeopardise its use. Here, we combined bulk solution MC‐ICP‐MS and in situ SIMS δ 56 Fe measurements on two Balmat batches: the Balmat‐Original published in Whitehouse and Fedo (2007) and Balmat‐UNIL. Despite similar compositions, this study demonstrates the existence of two isotopically distinct Balmat populations. With respect to Balmat‐Original (δ 56 Fe = ‐0.39 ± 0.05‰, 2 s ), Balmat‐UNIL is isotopically 'lighter' with a bulk solution MC‐ICP‐MS composition of ‐1.46 ± 0.024‰. Additionally, Balmat‐UNIL has two subpopulations: the first is characterised by δ 56 Fe values of ‐1.46 ± 0.25‰, whereas the second agrees with the original Balmat batch. In each Balmat‐UNIL subpopulation, the intra‐grain and inter‐grain variabilities are sufficient to use Balmat as a reference material for δ 56 Fe isotope measurements by SIMS. This study revealed at least two end‐member compositions of Balmat pyrite and calls for a careful batch‐specific determination of bulk δ 56 Fe.
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Pasquier et al. (2024) studied this question.
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